Bronchofiberscope, FB-19A
FDA 510(k) K770879 · Pilling Co.
510(k) numberK770879
Submission
- Device name
- Bronchofiberscope, FB-19A
- Applicant
- Pilling Co.
Mchenry, IL, US - Received
- May 16, 1977
- Decision date
- May 25, 1977
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
No product code recorded.
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Questions and answers
When was Bronchofiberscope, FB-19A cleared by the FDA?
Bronchofiberscope, FB-19A (K770879) received a 510(k) decision of Substantially Equivalent on May 25, 1977, 9 days after the submission was received.